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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21634Generated: October 29, 2026

Benzoyl chloride → N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine

https://huagongshe.com/reaction/21634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductN'-t-butyl-N-phenylacetyl-N'-benzoylhydrazineHCID 15451993—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a stirred suspension of t-butylhydrazine hydrochloride (2.0 g, 0.016M) in toluene (30 ml) was added 50% sodium hydroxide (1.3 g, 0.016M). After 15 minutes, the mixture was cooled to 5° C. and phenylacetyl chloride (2.4 g, 0.016M) and 50% sodium hydroxide (1.3 g, 0.016M) were added separately and simultaneously so as to maintain the reaction temperature below 10° C. After the addition, the reaction mixture was allowed to warm to room temperature and stirred for 1 hour. The mixture was diluted with hexane and the solid product isolated by filtration. This product (3.2 g, 0.015M) was dissolved in a stirred mixture of toluene (30 ml) and cooled on ice. To this mixture was added benzoylchloride (2.2 g, 0.016M) and 50% sodium hydroxide (1.3 g, 0.016M) simultaneously. After addition, the mixture was stirred for 1/2 hour, diluted with hexane and the solid product, N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine, isolated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424333
Source datasetuspto-grants-1995_06
ORD IDord-5d4415c8f6eb4a69a72e4f28887b0d14
Source noteuspto-grants-1995_06